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:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9B6Y7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006839 | mitochondrial transport | 4 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007005 | mitochondrion organization | 5 | 1 |
GO:0007006 | mitochondrial membrane organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0032978 | protein insertion into membrane from inner side | 6 | 1 |
GO:0032979 | protein insertion into mitochondrial inner membrane from matrix | 5 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051205 | protein insertion into membrane | 5 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0070585 | protein localization to mitochondrion | 6 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072655 | establishment of protein localization to mitochondrion | 5 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:0090151 | establishment of protein localization to mitochondrial membrane | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032977 | membrane insertase activity | 3 | 10 |
GO:0140104 | molecular carrier activity | 1 | 10 |
GO:0140597 | protein carrier chaperone | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.547 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 511 | 513 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.565 |
DEG_APCC_DBOX_1 | 144 | 152 | PF00400 | 0.634 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.497 |
DEG_SCF_FBW7_1 | 27 | 34 | PF00400 | 0.555 |
DEG_SPOP_SBC_1 | 225 | 229 | PF00917 | 0.367 |
DEG_SPOP_SBC_1 | 473 | 477 | PF00917 | 0.780 |
DOC_CDC14_PxL_1 | 242 | 250 | PF14671 | 0.485 |
DOC_CDC14_PxL_1 | 282 | 290 | PF14671 | 0.408 |
DOC_CKS1_1 | 439 | 444 | PF01111 | 0.593 |
DOC_CKS1_1 | 465 | 470 | PF01111 | 0.769 |
DOC_CYCLIN_yCln2_LP_2 | 238 | 244 | PF00134 | 0.361 |
DOC_CYCLIN_yCln2_LP_2 | 307 | 313 | PF00134 | 0.344 |
DOC_MAPK_FxFP_2 | 322 | 325 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 127 | 135 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 139 | 148 | PF00069 | 0.617 |
DOC_MAPK_MEF2A_6 | 292 | 299 | PF00069 | 0.308 |
DOC_PP1_RVXF_1 | 158 | 164 | PF00149 | 0.658 |
DOC_PP1_RVXF_1 | 269 | 276 | PF00149 | 0.531 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.591 |
DOC_PP2B_LxvP_1 | 236 | 239 | PF13499 | 0.356 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.369 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.521 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.581 |
DOC_PP4_FxxP_1 | 322 | 325 | PF00568 | 0.514 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.812 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.835 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.468 |
DOC_USP7_UBL2_3 | 511 | 515 | PF12436 | 0.820 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.781 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.806 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 336 | 342 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 349 | 354 | PF00244 | 0.764 |
LIG_14-3-3_CanoR_1 | 427 | 435 | PF00244 | 0.757 |
LIG_14-3-3_CanoR_1 | 70 | 77 | PF00244 | 0.416 |
LIG_Actin_WH2_2 | 298 | 316 | PF00022 | 0.346 |
LIG_AP2alpha_2 | 240 | 242 | PF02296 | 0.351 |
LIG_APCC_ABBA_1 | 133 | 138 | PF00400 | 0.406 |
LIG_BRCT_BRCA1_1 | 73 | 77 | PF00533 | 0.469 |
LIG_Clathr_ClatBox_1 | 254 | 258 | PF01394 | 0.344 |
LIG_deltaCOP1_diTrp_1 | 69 | 77 | PF00928 | 0.384 |
LIG_eIF4E_1 | 5 | 11 | PF01652 | 0.484 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.405 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.223 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.593 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.485 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.545 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.492 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.680 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.353 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.759 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.434 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.493 |
LIG_LIR_Gen_1 | 130 | 140 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 156 | 166 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 240 | 248 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 98 | 105 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.713 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.448 |
LIG_NRBOX | 394 | 400 | PF00104 | 0.690 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.352 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.480 |
LIG_SH2_GRB2like | 162 | 165 | PF00017 | 0.607 |
LIG_SH2_SRC | 298 | 301 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.648 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.763 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.415 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.765 |
LIG_SUMO_SIM_par_1 | 109 | 114 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 309 | 315 | PF11976 | 0.326 |
LIG_WRC_WIRS_1 | 288 | 293 | PF05994 | 0.528 |
MOD_CDK_SPK_2 | 10 | 15 | PF00069 | 0.450 |
MOD_CDK_SPK_2 | 331 | 336 | PF00069 | 0.678 |
MOD_CDK_SPK_2 | 477 | 482 | PF00069 | 0.627 |
MOD_CDK_SPxK_1 | 331 | 337 | PF00069 | 0.699 |
MOD_CDK_SPxxK_3 | 464 | 471 | PF00069 | 0.785 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.414 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.461 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.652 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.749 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.794 |
MOD_CK1_1 | 551 | 557 | PF00069 | 0.781 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.416 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.597 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.762 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.833 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.694 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.436 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.361 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.557 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.547 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.411 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.326 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.563 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.554 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.722 |
MOD_GlcNHglycan | 421 | 425 | PF01048 | 0.599 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.714 |
MOD_GlcNHglycan | 489 | 493 | PF01048 | 0.581 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.548 |
MOD_GlcNHglycan | 500 | 504 | PF01048 | 0.503 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.479 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.555 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.561 |
MOD_GlcNHglycan | 81 | 85 | PF01048 | 0.679 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.708 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.387 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.359 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.609 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.401 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.533 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.539 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.688 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.475 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.749 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.777 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.760 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.725 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.779 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.513 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.466 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.614 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.416 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.315 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.385 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.531 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.445 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.694 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.751 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.745 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.616 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.475 |
MOD_NEK2_2 | 370 | 375 | PF00069 | 0.669 |
MOD_PIKK_1 | 526 | 532 | PF00454 | 0.721 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.754 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.459 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.478 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.735 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.438 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.541 |
MOD_Plk_2-3 | 219 | 225 | PF00069 | 0.407 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.199 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.257 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.570 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.346 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.461 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.453 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.563 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.525 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.717 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.717 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.792 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.804 |
MOD_SUMO_rev_2 | 258 | 267 | PF00179 | 0.647 |
TRG_DiLeu_BaLyEn_6 | 307 | 312 | PF01217 | 0.344 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.738 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFR8 | Leptomonas seymouri | 55% | 100% |
A0A0S4JMC8 | Bodo saltans | 34% | 100% |
A0A3S7XA08 | Leishmania donovani | 88% | 100% |
A0A422P166 | Trypanosoma rangeli | 38% | 100% |
A4HNC5 | Leishmania braziliensis | 75% | 100% |
A4IBZ8 | Leishmania infantum | 89% | 100% |
E9AFT5 | Leishmania major | 87% | 100% |
V5BT14 | Trypanosoma cruzi | 38% | 100% |