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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4HHL7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006399 | tRNA metabolic process | 7 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008033 | tRNA processing | 8 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0034470 | ncRNA processing | 7 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0034660 | ncRNA metabolic process | 6 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016432 | tRNA-uridine aminocarboxypropyltransferase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 196 | 200 | PF00656 | 0.326 |
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.492 |
CLV_C14_Caspase3-7 | 487 | 491 | PF00656 | 0.449 |
CLV_MEL_PAP_1 | 396 | 402 | PF00089 | 0.240 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 575 | 577 | PF00675 | 0.759 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.640 |
CLV_PCSK_FUR_1 | 311 | 315 | PF00082 | 0.220 |
CLV_PCSK_FUR_1 | 486 | 490 | PF00082 | 0.457 |
CLV_PCSK_FUR_1 | 573 | 577 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.759 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 417 | 419 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.668 |
CLV_PCSK_PC7_1 | 489 | 495 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.529 |
CLV_Separin_Metazoa | 224 | 228 | PF03568 | 0.391 |
DEG_APCC_DBOX_1 | 464 | 472 | PF00400 | 0.301 |
DEG_APCC_DBOX_1 | 515 | 523 | PF00400 | 0.599 |
DEG_APCC_DBOX_1 | 596 | 604 | PF00400 | 0.514 |
DEG_COP1_1 | 563 | 571 | PF00400 | 0.479 |
DEG_SPOP_SBC_1 | 105 | 109 | PF00917 | 0.474 |
DEG_SPOP_SBC_1 | 18 | 22 | PF00917 | 0.404 |
DOC_CYCLIN_yCln2_LP_2 | 239 | 245 | PF00134 | 0.391 |
DOC_MAPK_DCC_7 | 132 | 141 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 157 | 166 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 168 | 174 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 372 | 379 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 83 | 89 | PF00069 | 0.639 |
DOC_MAPK_MEF2A_6 | 132 | 141 | PF00069 | 0.608 |
DOC_MAPK_MEF2A_6 | 395 | 404 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 500 | 508 | PF00069 | 0.382 |
DOC_PP2B_LxvP_1 | 239 | 242 | PF13499 | 0.391 |
DOC_PP2B_LxvP_1 | 517 | 520 | PF13499 | 0.614 |
DOC_PP4_FxxP_1 | 571 | 574 | PF00568 | 0.667 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.542 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.341 |
LIG_14-3-3_CanoR_1 | 161 | 167 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 168 | 173 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 202 | 206 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 340 | 344 | PF00244 | 0.240 |
LIG_14-3-3_CanoR_1 | 399 | 403 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 545 | 555 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 56 | 64 | PF00244 | 0.536 |
LIG_Actin_WH2_2 | 455 | 471 | PF00022 | 0.438 |
LIG_APCC_ABBA_1 | 218 | 223 | PF00400 | 0.357 |
LIG_CaM_NSCaTE_8 | 149 | 156 | PF13499 | 0.307 |
LIG_Clathr_ClatBox_1 | 376 | 380 | PF01394 | 0.391 |
LIG_deltaCOP1_diTrp_1 | 148 | 152 | PF00928 | 0.455 |
LIG_EH1_1 | 31 | 39 | PF00400 | 0.298 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.531 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.357 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.492 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.410 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.431 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.534 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.682 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.318 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.492 |
LIG_FHA_2 | 547 | 553 | PF00498 | 0.648 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.595 |
LIG_HP1_1 | 398 | 402 | PF01393 | 0.391 |
LIG_IBAR_NPY_1 | 28 | 30 | PF08397 | 0.485 |
LIG_LIR_Apic_2 | 570 | 574 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 406 | 415 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.334 |
LIG_PTB_Apo_2 | 521 | 528 | PF02174 | 0.504 |
LIG_PTB_Phospho_1 | 521 | 527 | PF10480 | 0.510 |
LIG_SH2_CRK | 291 | 295 | PF00017 | 0.240 |
LIG_SH2_CRK | 336 | 340 | PF00017 | 0.240 |
LIG_SH2_SRC | 291 | 294 | PF00017 | 0.240 |
LIG_SH2_SRC | 470 | 473 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 408 | 412 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 443 | 447 | PF00017 | 0.438 |
LIG_SH2_STAT3 | 254 | 257 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 300 | 303 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.427 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.365 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.582 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.690 |
LIG_SUMO_SIM_par_1 | 375 | 382 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 563 | 570 | PF11976 | 0.476 |
LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.624 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.240 |
LIG_TRAF2_1 | 57 | 60 | PF00917 | 0.639 |
LIG_UBA3_1 | 411 | 417 | PF00899 | 0.357 |
MOD_CDK_SPK_2 | 316 | 321 | PF00069 | 0.240 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.773 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.438 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.448 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.399 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.623 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.557 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.739 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.615 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.357 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.598 |
MOD_CK2_1 | 546 | 552 | PF00069 | 0.650 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.733 |
MOD_Cter_Amidation | 578 | 581 | PF01082 | 0.519 |
MOD_GlcNHglycan | 123 | 127 | PF01048 | 0.720 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.681 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.475 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.436 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.592 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.553 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.700 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.723 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.571 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.566 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.475 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.473 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.381 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.527 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.651 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.580 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.534 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.356 |
MOD_N-GLC_2 | 524 | 526 | PF02516 | 0.463 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.417 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.595 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.358 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.279 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.240 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.391 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.357 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.326 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.623 |
MOD_NEK2_2 | 277 | 282 | PF00069 | 0.438 |
MOD_PIKK_1 | 299 | 305 | PF00454 | 0.376 |
MOD_PIKK_1 | 602 | 608 | PF00454 | 0.740 |
MOD_PK_1 | 168 | 174 | PF00069 | 0.534 |
MOD_PKA_1 | 168 | 174 | PF00069 | 0.418 |
MOD_PKA_1 | 416 | 422 | PF00069 | 0.357 |
MOD_PKA_1 | 92 | 98 | PF00069 | 0.569 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.418 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.532 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.492 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.357 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.240 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.492 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.666 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.518 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.597 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.374 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.391 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.357 |
MOD_Plk_1 | 581 | 587 | PF00069 | 0.527 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.573 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.498 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.351 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.365 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.357 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.492 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.341 |
MOD_SUMO_for_1 | 156 | 159 | PF00179 | 0.343 |
MOD_SUMO_for_1 | 320 | 323 | PF00179 | 0.386 |
MOD_SUMO_for_1 | 71 | 74 | PF00179 | 0.439 |
MOD_SUMO_rev_2 | 142 | 152 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_1 | 215 | 220 | PF01217 | 0.438 |
TRG_DiLeu_BaEn_2 | 147 | 153 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 392 | 397 | PF01217 | 0.240 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.240 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.332 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 311 | 314 | PF00400 | 0.239 |
TRG_ER_diArg_1 | 415 | 418 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 485 | 488 | PF00400 | 0.367 |
TRG_ER_diArg_1 | 515 | 518 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 573 | 576 | PF00400 | 0.738 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.584 |
TRG_NES_CRM1_1 | 208 | 224 | PF08389 | 0.240 |
TRG_NLS_MonoExtC_3 | 415 | 420 | PF00514 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6V5 | Leptomonas seymouri | 55% | 100% |
A0A0S4JPN0 | Bodo saltans | 37% | 100% |
A0A3Q8IHF3 | Leishmania donovani | 75% | 100% |
A4I4S6 | Leishmania infantum | 75% | 100% |
C9ZLH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AE79 | Leishmania major | 75% | 100% |
E9ALK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |