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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4HD65
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 104 | 108 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.428 |
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 396 | 400 | PF00656 | 0.658 |
CLV_C14_Caspase3-7 | 76 | 80 | PF00656 | 0.441 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.781 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.400 |
CLV_PCSK_PC7_1 | 388 | 394 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.720 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.544 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.521 |
DOC_MAPK_MEF2A_6 | 411 | 418 | PF00069 | 0.595 |
DOC_MAPK_NFAT4_5 | 411 | 419 | PF00069 | 0.609 |
DOC_MAPK_RevD_3 | 60 | 75 | PF00069 | 0.373 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.636 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.442 |
LIG_14-3-3_CanoR_1 | 130 | 139 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 227 | 234 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 392 | 398 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 74 | 78 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 89 | 93 | PF00244 | 0.364 |
LIG_Actin_WH2_2 | 174 | 190 | PF00022 | 0.448 |
LIG_APCC_ABBA_1 | 333 | 338 | PF00400 | 0.378 |
LIG_BH_BH3_1 | 4 | 20 | PF00452 | 0.364 |
LIG_BIR_III_4 | 79 | 83 | PF00653 | 0.456 |
LIG_EH1_1 | 324 | 332 | PF00400 | 0.349 |
LIG_EVH1_2 | 254 | 258 | PF00568 | 0.432 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.458 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.434 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.428 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.539 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.473 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.374 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.649 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.575 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.400 |
LIG_LIR_Gen_1 | 24 | 30 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 320 | 331 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 85 | 94 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 134 | 139 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 24 | 28 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 43 | 47 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.333 |
LIG_NRBOX | 66 | 72 | PF00104 | 0.355 |
LIG_Pex14_2 | 380 | 384 | PF04695 | 0.603 |
LIG_SH2_PTP2 | 136 | 139 | PF00017 | 0.495 |
LIG_SH2_PTP2 | 323 | 326 | PF00017 | 0.344 |
LIG_SH2_SRC | 126 | 129 | PF00017 | 0.426 |
LIG_SH2_SRC | 136 | 139 | PF00017 | 0.443 |
LIG_SH2_SRC | 94 | 97 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.591 |
LIG_SH2_STAT3 | 372 | 375 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.347 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.372 |
LIG_SUMO_SIM_anti_2 | 277 | 283 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 204 | 210 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 60 | 65 | PF11976 | 0.390 |
LIG_TRAF2_1 | 219 | 222 | PF00917 | 0.599 |
LIG_TYR_ITIM | 321 | 326 | PF00017 | 0.344 |
LIG_TYR_ITIM | 49 | 54 | PF00017 | 0.356 |
LIG_TYR_ITIM | 92 | 97 | PF00017 | 0.355 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.486 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.465 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.500 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.415 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.631 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.746 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.499 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.511 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.698 |
MOD_N-GLC_1 | 306 | 311 | PF02516 | 0.636 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.475 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.520 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.374 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.370 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.362 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.428 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.371 |
MOD_NEK2_2 | 186 | 191 | PF00069 | 0.467 |
MOD_PIKK_1 | 120 | 126 | PF00454 | 0.361 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.607 |
MOD_PKA_1 | 227 | 233 | PF00069 | 0.423 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.543 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.488 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.477 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.586 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.623 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.630 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.377 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.365 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.296 |
MOD_Plk_2-3 | 409 | 415 | PF00069 | 0.516 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.445 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.291 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.641 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.449 |
MOD_SUMO_for_1 | 315 | 318 | PF00179 | 0.455 |
MOD_SUMO_for_1 | 40 | 43 | PF00179 | 0.499 |
MOD_SUMO_rev_2 | 104 | 111 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 196 | 200 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 29 | 35 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 310 | 315 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 404 | 412 | PF00179 | 0.669 |
MOD_SUMO_rev_2 | 413 | 419 | PF00179 | 0.648 |
TRG_DiLeu_BaEn_1 | 170 | 175 | PF01217 | 0.427 |
TRG_DiLeu_BaEn_1 | 213 | 218 | PF01217 | 0.457 |
TRG_DiLeu_LyEn_5 | 213 | 218 | PF01217 | 0.396 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.679 |
TRG_Pf-PMV_PEXEL_1 | 216 | 221 | PF00026 | 0.694 |
TRG_Pf-PMV_PEXEL_1 | 267 | 271 | PF00026 | 0.720 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3N9 | Leptomonas seymouri | 76% | 99% |
A0A0S4IV95 | Bodo saltans | 54% | 100% |
A0A1X0NKJ2 | Trypanosomatidae | 63% | 99% |
A0A3Q8ICV4 | Leishmania donovani | 81% | 100% |
A4I0N0 | Leishmania infantum | 82% | 100% |
D0A6X8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 99% |
E9AWJ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QAX3 | Leishmania major | 82% | 100% |
V5BW05 | Trypanosoma cruzi | 63% | 94% |