Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0070761 | pre-snoRNP complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HG71
Term | Name | Level | Count |
---|---|---|---|
GO:0000463 | maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000470 | maturation of LSU-rRNA | 9 | 1 |
GO:0000491 | small nucleolar ribonucleoprotein complex assembly | 7 | 1 |
GO:0000492 | box C/D snoRNP assembly | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006403 | RNA localization | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048254 | snoRNA localization | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 348 | 352 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 404 | 408 | PF00656 | 0.778 |
CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.748 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.433 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 539 | 541 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 612 | 614 | PF00082 | 0.459 |
CLV_PCSK_PC7_1 | 231 | 237 | PF00082 | 0.484 |
CLV_PCSK_PC7_1 | 553 | 559 | PF00082 | 0.450 |
CLV_PCSK_PC7_1 | 608 | 614 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 584 | 588 | PF00082 | 0.337 |
DEG_APCC_DBOX_1 | 292 | 300 | PF00400 | 0.335 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.537 |
DEG_SCF_FBW7_2 | 121 | 127 | PF00400 | 0.579 |
DEG_SCF_FBW7_2 | 429 | 436 | PF00400 | 0.410 |
DEG_SCF_TRCP1_1 | 69 | 74 | PF00400 | 0.526 |
DOC_CKS1_1 | 121 | 126 | PF01111 | 0.513 |
DOC_CKS1_1 | 430 | 435 | PF01111 | 0.474 |
DOC_CKS1_1 | 437 | 442 | PF01111 | 0.426 |
DOC_CYCLIN_RxL_1 | 557 | 569 | PF00134 | 0.310 |
DOC_CYCLIN_yCln2_LP_2 | 223 | 229 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 434 | 440 | PF00134 | 0.454 |
DOC_PP1_RVXF_1 | 484 | 491 | PF00149 | 0.329 |
DOC_PP2B_LxvP_1 | 223 | 226 | PF13499 | 0.391 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.605 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.490 |
LIG_14-3-3_CanoR_1 | 132 | 139 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 143 | 149 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 153 | 159 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 213 | 217 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 507 | 511 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 520 | 524 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 538 | 545 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 597 | 601 | PF00244 | 0.344 |
LIG_14-3-3_CterR_2 | 658 | 662 | PF00244 | 0.673 |
LIG_AP2alpha_2 | 90 | 92 | PF02296 | 0.487 |
LIG_APCC_ABBA_1 | 161 | 166 | PF00400 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 277 | 289 | PF00928 | 0.339 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.359 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.431 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.378 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.469 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.652 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.657 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.758 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.806 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.498 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.330 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.391 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.488 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.495 |
LIG_LIR_Gen_1 | 193 | 198 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 279 | 288 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 476 | 485 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 193 | 197 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 219 | 223 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 456 | 460 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 476 | 481 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 493 | 497 | PF02991 | 0.298 |
LIG_Pex14_1 | 216 | 220 | PF04695 | 0.493 |
LIG_Pex14_1 | 267 | 271 | PF04695 | 0.325 |
LIG_Pex14_2 | 448 | 452 | PF04695 | 0.438 |
LIG_Pex14_2 | 490 | 494 | PF04695 | 0.311 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.368 |
LIG_SH2_CRK | 220 | 224 | PF00017 | 0.548 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.412 |
LIG_SH2_NCK_1 | 146 | 150 | PF00017 | 0.368 |
LIG_SH2_NCK_1 | 426 | 430 | PF00017 | 0.526 |
LIG_SH2_SRC | 426 | 429 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.296 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.508 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.707 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.579 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.499 |
LIG_SH3_3 | 653 | 659 | PF00018 | 0.517 |
LIG_SxIP_EBH_1 | 573 | 584 | PF03271 | 0.288 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.672 |
LIG_TRAF2_1 | 408 | 411 | PF00917 | 0.744 |
LIG_TRAF2_1 | 425 | 428 | PF00917 | 0.438 |
LIG_TRAF2_1 | 439 | 442 | PF00917 | 0.311 |
LIG_TRFH_1 | 473 | 477 | PF08558 | 0.419 |
LIG_WW_3 | 655 | 659 | PF00397 | 0.575 |
MOD_CDK_SPK_2 | 117 | 122 | PF00069 | 0.507 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.617 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.414 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.589 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.604 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.788 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.782 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.597 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.434 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.378 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.277 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.468 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.472 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.673 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.532 |
MOD_Cter_Amidation | 151 | 154 | PF01082 | 0.464 |
MOD_GlcNHglycan | 100 | 105 | PF01048 | 0.559 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.565 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.487 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.647 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.700 |
MOD_GlcNHglycan | 363 | 367 | PF01048 | 0.698 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.639 |
MOD_GlcNHglycan | 60 | 64 | PF01048 | 0.698 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.509 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.511 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.681 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.566 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.724 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.290 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.463 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.461 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.684 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.614 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.652 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.737 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.501 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.395 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.628 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.658 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.475 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.338 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.517 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.252 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.523 |
MOD_NEK2_2 | 596 | 601 | PF00069 | 0.279 |
MOD_OFUCOSY | 151 | 156 | PF10250 | 0.358 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.600 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.351 |
MOD_PKA_1 | 132 | 138 | PF00069 | 0.349 |
MOD_PKA_1 | 538 | 544 | PF00069 | 0.576 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.369 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.477 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.516 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.392 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.634 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.782 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.477 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.379 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.449 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.313 |
MOD_PKB_1 | 536 | 544 | PF00069 | 0.389 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.393 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.462 |
MOD_Plk_2-3 | 616 | 622 | PF00069 | 0.394 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.387 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.563 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.659 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.523 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.483 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.492 |
MOD_SUMO_rev_2 | 166 | 171 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 253 | 262 | PF00179 | 0.531 |
MOD_SUMO_rev_2 | 513 | 518 | PF00179 | 0.467 |
TRG_DiLeu_BaEn_2 | 492 | 498 | PF01217 | 0.422 |
TRG_DiLeu_BaEn_4 | 546 | 552 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 306 | 311 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 430 | 435 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.652 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 485 | 487 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 534 | 537 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 557 | 559 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 625 | 628 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 657 | 660 | PF00400 | 0.717 |
TRG_NES_CRM1_1 | 479 | 493 | PF08389 | 0.384 |
TRG_NLS_MonoExtC_3 | 610 | 615 | PF00514 | 0.451 |
TRG_NLS_MonoExtN_4 | 608 | 615 | PF00514 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 563 | 568 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0N9 | Leptomonas seymouri | 58% | 100% |
A0A3Q8IQB2 | Leishmania donovani | 78% | 100% |
A0A422N6T6 | Trypanosoma rangeli | 45% | 100% |
A4I3B4 | Leishmania infantum | 78% | 100% |
D0A7T3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AZJ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q8P0 | Leishmania major | 77% | 100% |
V5BJ07 | Trypanosoma cruzi | 47% | 100% |