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: A0A3Q8IQB2
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 | 30 | 34 | PF00656 | 0.756 |
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.774 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.493 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 509 | 511 | PF00082 | 0.645 |
CLV_PCSK_PC1ET2_1 | 582 | 584 | PF00082 | 0.520 |
CLV_PCSK_PC7_1 | 200 | 206 | PF00082 | 0.521 |
CLV_PCSK_PC7_1 | 523 | 529 | PF00082 | 0.583 |
CLV_PCSK_PC7_1 | 578 | 584 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.775 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.396 |
DEG_APCC_DBOX_1 | 261 | 269 | PF00400 | 0.400 |
DEG_SCF_FBW7_1 | 316 | 321 | PF00400 | 0.602 |
DEG_SCF_FBW7_2 | 89 | 96 | PF00400 | 0.652 |
DOC_CKS1_1 | 406 | 411 | PF01111 | 0.509 |
DOC_CYCLIN_yCln2_LP_2 | 192 | 198 | PF00134 | 0.446 |
DOC_CYCLIN_yCln2_LP_2 | 383 | 389 | PF00134 | 0.752 |
DOC_MAPK_gen_1 | 122 | 130 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 123 | 132 | PF00069 | 0.551 |
DOC_MAPK_MEF2A_6 | 143 | 151 | PF00069 | 0.297 |
DOC_MAPK_MEF2A_6 | 393 | 401 | PF00069 | 0.631 |
DOC_PP1_RVXF_1 | 454 | 461 | PF00149 | 0.391 |
DOC_PP2B_LxvP_1 | 192 | 195 | PF13499 | 0.455 |
DOC_PP2B_LxvP_1 | 383 | 386 | PF13499 | 0.760 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.540 |
DOC_PP4_FxxP_1 | 625 | 628 | PF00568 | 0.727 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.627 |
DOC_USP7_UBL2_3 | 134 | 138 | PF12436 | 0.518 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 590 | 595 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.783 |
LIG_14-3-3_CanoR_1 | 122 | 128 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 182 | 186 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 477 | 481 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 490 | 494 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 508 | 515 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 567 | 571 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 73 | 81 | PF00244 | 0.643 |
LIG_14-3-3_CterR_2 | 629 | 633 | PF00244 | 0.776 |
LIG_APCC_ABBA_1 | 130 | 135 | PF00400 | 0.647 |
LIG_BIR_III_4 | 14 | 18 | PF00653 | 0.555 |
LIG_EVH1_1 | 399 | 403 | PF00568 | 0.602 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.481 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.413 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.778 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.724 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.826 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.476 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.624 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.630 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.393 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.450 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.540 |
LIG_LIR_Gen_1 | 162 | 167 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 425 | 433 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 446 | 455 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 555 | 563 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 162 | 166 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 446 | 451 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 462 | 467 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 555 | 559 | PF02991 | 0.423 |
LIG_Pex14_1 | 185 | 189 | PF04695 | 0.544 |
LIG_Pex14_1 | 236 | 240 | PF04695 | 0.387 |
LIG_Pex14_2 | 417 | 421 | PF04695 | 0.574 |
LIG_Pex14_2 | 460 | 464 | PF04695 | 0.355 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.490 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.595 |
LIG_SH2_CRK | 448 | 452 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 115 | 119 | PF00017 | 0.490 |
LIG_SH2_NCK_1 | 288 | 292 | PF00017 | 0.539 |
LIG_SH2_PTP2 | 427 | 430 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 395 | 399 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.716 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.730 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.448 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.714 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.588 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.510 |
LIG_SUMO_SIM_anti_2 | 340 | 347 | PF11976 | 0.604 |
LIG_TRFH_1 | 443 | 447 | PF08558 | 0.481 |
MOD_CDC14_SPxK_1 | 593 | 596 | PF00782 | 0.570 |
MOD_CDK_SPK_2 | 405 | 410 | PF00069 | 0.475 |
MOD_CDK_SPxK_1 | 590 | 596 | PF00069 | 0.565 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.617 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.473 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.790 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.649 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.644 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.674 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.664 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.492 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.420 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.401 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.547 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.532 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.699 |
MOD_Cter_Amidation | 120 | 123 | PF01082 | 0.347 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.621 |
MOD_GlcNHglycan | 28 | 32 | PF01048 | 0.731 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.781 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.767 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.750 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.555 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.660 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.594 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.530 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.781 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.569 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.735 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.773 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.642 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.718 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.457 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.783 |
MOD_N-GLC_1 | 590 | 595 | PF02516 | 0.520 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.595 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.761 |
MOD_OFUCOSY | 120 | 125 | PF10250 | 0.290 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.691 |
MOD_PKA_1 | 508 | 514 | PF00069 | 0.632 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.561 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.770 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.566 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.450 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.586 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.547 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.390 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.519 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.373 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.713 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.517 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.455 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.531 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.674 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.662 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.498 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.583 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.450 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.606 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.486 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.547 |
MOD_ProDKin_1 | 590 | 596 | PF00069 | 0.565 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.781 |
MOD_SUMO_rev_2 | 135 | 140 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 222 | 231 | PF00179 | 0.573 |
MOD_SUMO_rev_2 | 483 | 488 | PF00179 | 0.583 |
TRG_DiLeu_BaEn_2 | 462 | 468 | PF01217 | 0.464 |
TRG_DiLeu_BaEn_4 | 516 | 522 | PF01217 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 275 | 280 | PF01217 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 607 | 612 | PF01217 | 0.555 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.670 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 262 | 265 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 507 | 510 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 527 | 529 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 595 | 598 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 628 | 631 | PF00400 | 0.743 |
TRG_NES_CRM1_1 | 449 | 463 | PF08389 | 0.442 |
TRG_NLS_MonoExtC_3 | 580 | 585 | PF00514 | 0.512 |
TRG_NLS_MonoExtN_4 | 578 | 585 | PF00514 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 157 | 162 | PF00026 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 533 | 538 | PF00026 | 0.508 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0N9 | Leptomonas seymouri | 58% | 100% |
A0A422N6T6 | Trypanosoma rangeli | 46% | 100% |
A4HG71 | Leishmania braziliensis | 78% | 100% |
A4I3B4 | Leishmania infantum | 100% | 100% |
D0A7T3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AZJ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q8P0 | Leishmania major | 91% | 100% |
V5BJ07 | Trypanosoma cruzi | 47% | 100% |