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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QH51
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.529 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.691 |
CLV_PCSK_FUR_1 | 223 | 227 | PF00082 | 0.630 |
CLV_PCSK_FUR_1 | 352 | 356 | PF00082 | 0.653 |
CLV_PCSK_FUR_1 | 36 | 40 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.704 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.573 |
CLV_PCSK_PC7_1 | 340 | 346 | PF00082 | 0.639 |
CLV_PCSK_PC7_1 | 426 | 432 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.557 |
CLV_Separin_Metazoa | 441 | 445 | PF03568 | 0.543 |
DEG_APCC_DBOX_1 | 344 | 352 | PF00400 | 0.552 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.481 |
DEG_SCF_FBW7_1 | 101 | 106 | PF00400 | 0.651 |
DEG_SPOP_SBC_1 | 396 | 400 | PF00917 | 0.480 |
DOC_ANK_TNKS_1 | 354 | 361 | PF00023 | 0.681 |
DOC_CKS1_1 | 237 | 242 | PF01111 | 0.696 |
DOC_CYCLIN_RxL_1 | 306 | 315 | PF00134 | 0.694 |
DOC_MAPK_MEF2A_6 | 3 | 12 | PF00069 | 0.485 |
DOC_PP2B_LxvP_1 | 95 | 98 | PF13499 | 0.701 |
DOC_PP4_FxxP_1 | 237 | 240 | PF00568 | 0.702 |
DOC_PP4_FxxP_1 | 347 | 350 | PF00568 | 0.623 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.800 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.553 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.820 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.604 |
LIG_14-3-3_CanoR_1 | 214 | 221 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 444 | 449 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 92 | 98 | PF00244 | 0.604 |
LIG_Clathr_ClatBox_1 | 311 | 315 | PF01394 | 0.678 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.670 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.570 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.674 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.754 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.577 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.649 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.514 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.534 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.726 |
LIG_Integrin_RGD_1 | 355 | 357 | PF01839 | 0.565 |
LIG_LIR_Apic_2 | 336 | 341 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 381 | 391 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 381 | 386 | PF02991 | 0.703 |
LIG_MYND_1 | 346 | 350 | PF01753 | 0.670 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.668 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.577 |
LIG_SH2_NCK_1 | 338 | 342 | PF00017 | 0.619 |
LIG_SH2_STAP1 | 383 | 387 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.522 |
LIG_SH3_1 | 414 | 420 | PF00018 | 0.581 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.787 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.533 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.713 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.681 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.627 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.583 |
LIG_TRFH_1 | 312 | 316 | PF08558 | 0.675 |
LIG_UBA3_1 | 253 | 261 | PF00899 | 0.467 |
LIG_WRC_WIRS_1 | 172 | 177 | PF05994 | 0.591 |
LIG_WRC_WIRS_1 | 445 | 450 | PF05994 | 0.566 |
MOD_CDC14_SPxK_1 | 145 | 148 | PF00782 | 0.680 |
MOD_CDK_SPK_2 | 236 | 241 | PF00069 | 0.655 |
MOD_CDK_SPxK_1 | 142 | 148 | PF00069 | 0.677 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.756 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.613 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.659 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.613 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.718 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.612 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.679 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.808 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.559 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.676 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.610 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.774 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.601 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.535 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.576 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.691 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.600 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.750 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.749 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.565 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.586 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.775 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.514 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.691 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.711 |
MOD_GlcNHglycan | 359 | 363 | PF01048 | 0.679 |
MOD_GlcNHglycan | 432 | 436 | PF01048 | 0.548 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.761 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.662 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.574 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.616 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.646 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.652 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.615 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.698 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.627 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.664 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.580 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.658 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.637 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.505 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.529 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.634 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.633 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.454 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.465 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.686 |
MOD_PKA_1 | 225 | 231 | PF00069 | 0.623 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.754 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.694 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.665 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.607 |
MOD_PKB_1 | 223 | 231 | PF00069 | 0.628 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.678 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.578 |
MOD_Plk_2-3 | 171 | 177 | PF00069 | 0.639 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.683 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.605 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.563 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.577 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.722 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.629 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.638 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.626 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.820 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.604 |
MOD_SUMO_rev_2 | 458 | 463 | PF00179 | 0.672 |
TRG_DiLeu_BaEn_2 | 373 | 379 | PF01217 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 4 | 9 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.590 |
TRG_ER_diArg_1 | 223 | 226 | PF00400 | 0.722 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 344 | 346 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.529 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HV85 | Leptomonas seymouri | 26% | 100% |
A0A3S7WRI4 | Leishmania donovani | 88% | 100% |
A4H9S9 | Leishmania braziliensis | 58% | 93% |
A4HUU0 | Leishmania infantum | 88% | 100% |
E9ANH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 97% |