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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3Q8IPV2
PDB structure(s): 7ane_q
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.354 |
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.687 |
CLV_C14_Caspase3-7 | 337 | 341 | PF00656 | 0.621 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.551 |
CLV_PCSK_FUR_1 | 100 | 104 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.669 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.675 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.438 |
CLV_PCSK_PC7_1 | 282 | 288 | PF00082 | 0.544 |
CLV_PCSK_PC7_1 | 58 | 64 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.627 |
DOC_CKS1_1 | 31 | 36 | PF01111 | 0.428 |
DOC_CYCLIN_RxL_1 | 112 | 125 | PF00134 | 0.458 |
DOC_MAPK_gen_1 | 116 | 122 | PF00069 | 0.455 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.651 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.434 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.663 |
DOC_USP7_UBL2_3 | 294 | 298 | PF12436 | 0.615 |
DOC_USP7_UBL2_3 | 345 | 349 | PF12436 | 0.723 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.676 |
LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 400 | 407 | PF00244 | 0.615 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.455 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.669 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.659 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.525 |
LIG_LIR_Apic_2 | 214 | 219 | PF02991 | 0.633 |
LIG_LIR_Apic_2 | 29 | 34 | PF02991 | 0.435 |
LIG_LIR_Apic_2 | 299 | 304 | PF02991 | 0.687 |
LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.420 |
LIG_MYND_3 | 183 | 187 | PF01753 | 0.499 |
LIG_MYND_3 | 379 | 383 | PF01753 | 0.677 |
LIG_PDZ_Class_3 | 421 | 426 | PF00595 | 0.661 |
LIG_Pex14_1 | 65 | 69 | PF04695 | 0.409 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.473 |
LIG_SH2_GRB2like | 15 | 18 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 135 | 139 | PF00017 | 0.401 |
LIG_SH2_NCK_1 | 16 | 20 | PF00017 | 0.458 |
LIG_SH2_NCK_1 | 216 | 220 | PF00017 | 0.669 |
LIG_SH2_STAT3 | 150 | 153 | PF00017 | 0.486 |
LIG_SH2_STAT3 | 61 | 64 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.409 |
LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.589 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.597 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.617 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.634 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.614 |
LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.410 |
MOD_CDK_SPxK_1 | 30 | 36 | PF00069 | 0.440 |
MOD_CDK_SPxK_1 | 317 | 323 | PF00069 | 0.692 |
MOD_CDK_SPxxK_3 | 317 | 324 | PF00069 | 0.688 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.490 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.671 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.596 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.529 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.614 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.624 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.633 |
MOD_Cter_Amidation | 24 | 27 | PF01082 | 0.506 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.552 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.706 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.673 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.724 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.538 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.572 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.564 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.446 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.549 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.588 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.697 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.667 |
MOD_LATS_1 | 24 | 30 | PF00433 | 0.483 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.418 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.614 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.539 |
MOD_NEK2_2 | 211 | 216 | PF00069 | 0.629 |
MOD_NEK2_2 | 296 | 301 | PF00069 | 0.631 |
MOD_NEK2_2 | 65 | 70 | PF00069 | 0.411 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.574 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.509 |
MOD_PKA_1 | 102 | 108 | PF00069 | 0.574 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.465 |
MOD_PKA_1 | 324 | 330 | PF00069 | 0.701 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.574 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.405 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.547 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.570 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.701 |
MOD_PKB_1 | 100 | 108 | PF00069 | 0.637 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.691 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.633 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.658 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.440 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.758 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.482 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.672 |
MOD_SUMO_for_1 | 351 | 354 | PF00179 | 0.732 |
MOD_SUMO_rev_2 | 220 | 230 | PF00179 | 0.663 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.468 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.702 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.679 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.625 |
TRG_NLS_Bipartite_1 | 100 | 120 | PF00514 | 0.487 |
TRG_NLS_MonoCore_2 | 322 | 327 | PF00514 | 0.681 |
TRG_NLS_MonoExtC_3 | 115 | 121 | PF00514 | 0.462 |
TRG_NLS_MonoExtC_3 | 324 | 330 | PF00514 | 0.604 |
TRG_NLS_MonoExtN_4 | 321 | 327 | PF00514 | 0.631 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2P6 | Leptomonas seymouri | 78% | 100% |
A0A0S4IKL5 | Bodo saltans | 51% | 91% |
A0A1X0P5A6 | Trypanosomatidae | 61% | 96% |
A0A3R7NKQ1 | Trypanosoma rangeli | 62% | 97% |
A4HN18 | Leishmania braziliensis | 93% | 100% |
A4IBN9 | Leishmania infantum | 100% | 100% |
C9ZYZ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 97% |
E9AFH3 | Leishmania major | 97% | 100% |
E9B6M8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
V5BY99 | Trypanosoma cruzi | 61% | 96% |