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: A4HJ47
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.577 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.504 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.536 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.559 |
DOC_CKS1_1 | 114 | 119 | PF01111 | 0.646 |
DOC_CKS1_1 | 135 | 140 | PF01111 | 0.649 |
DOC_CYCLIN_yCln2_LP_2 | 379 | 385 | PF00134 | 0.553 |
DOC_MAPK_DCC_7 | 414 | 423 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 303 | 311 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 299 | 306 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 414 | 423 | PF00069 | 0.541 |
DOC_MAPK_NFAT4_5 | 299 | 307 | PF00069 | 0.431 |
DOC_PP2B_LxvP_1 | 194 | 197 | PF13499 | 0.518 |
DOC_PP2B_LxvP_1 | 379 | 382 | PF13499 | 0.548 |
DOC_PP4_FxxP_1 | 102 | 105 | PF00568 | 0.421 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.694 |
DOC_PP4_MxPP_1 | 423 | 426 | PF00568 | 0.682 |
DOC_SPAK_OSR1_1 | 101 | 105 | PF12202 | 0.458 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.481 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 218 | 224 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 299 | 303 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 55 | 64 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 72 | 79 | PF00244 | 0.636 |
LIG_Actin_WH2_2 | 189 | 204 | PF00022 | 0.521 |
LIG_BIR_III_4 | 10 | 14 | PF00653 | 0.610 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.678 |
LIG_CSL_BTD_1 | 317 | 320 | PF09270 | 0.599 |
LIG_deltaCOP1_diTrp_1 | 91 | 102 | PF00928 | 0.426 |
LIG_EVH1_2 | 189 | 193 | PF00568 | 0.502 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.640 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.430 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.467 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.568 |
LIG_LIR_Apic_2 | 137 | 142 | PF02991 | 0.616 |
LIG_LIR_Apic_2 | 186 | 190 | PF02991 | 0.549 |
LIG_LIR_Apic_2 | 253 | 257 | PF02991 | 0.396 |
LIG_LIR_Apic_2 | 337 | 343 | PF02991 | 0.584 |
LIG_LIR_Apic_2 | 476 | 481 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 14 | 24 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 192 | 201 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 417 | 427 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 58 | 69 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 93 | 104 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 473 | 478 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.479 |
LIG_LYPXL_yS_3 | 231 | 234 | PF13949 | 0.527 |
LIG_MYND_1 | 106 | 110 | PF01753 | 0.467 |
LIG_NRBOX | 375 | 381 | PF00104 | 0.539 |
LIG_NRP_CendR_1 | 483 | 484 | PF00754 | 0.611 |
LIG_Pex14_1 | 96 | 100 | PF04695 | 0.470 |
LIG_PTB_Apo_2 | 94 | 101 | PF02174 | 0.471 |
LIG_SH2_CRK | 139 | 143 | PF00017 | 0.689 |
LIG_SH2_CRK | 187 | 191 | PF00017 | 0.502 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.423 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.680 |
LIG_SH2_NCK_1 | 139 | 143 | PF00017 | 0.538 |
LIG_SH2_NCK_1 | 187 | 191 | PF00017 | 0.502 |
LIG_SH2_NCK_1 | 359 | 363 | PF00017 | 0.511 |
LIG_SH2_PTP2 | 16 | 19 | PF00017 | 0.415 |
LIG_SH2_PTP2 | 45 | 48 | PF00017 | 0.393 |
LIG_SH2_SRC | 16 | 19 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 252 | 256 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.687 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.393 |
LIG_SH3_1 | 139 | 145 | PF00018 | 0.538 |
LIG_SH3_2 | 197 | 202 | PF14604 | 0.532 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.453 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.569 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.618 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.667 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.678 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.532 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.664 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.695 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.661 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.645 |
LIG_SUMO_SIM_anti_2 | 275 | 282 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 275 | 282 | PF11976 | 0.552 |
LIG_TRAF2_1 | 85 | 88 | PF00917 | 0.600 |
MOD_CDC14_SPxK_1 | 199 | 202 | PF00782 | 0.537 |
MOD_CDK_SPxK_1 | 196 | 202 | PF00069 | 0.530 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.752 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.576 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.605 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.680 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.566 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.549 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.531 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.717 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.616 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.548 |
MOD_GlcNHglycan | 179 | 183 | PF01048 | 0.611 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.699 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.648 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.662 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.604 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.488 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.481 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.593 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.628 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.658 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.582 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.775 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.577 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.618 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.586 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.495 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.643 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.500 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.543 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.611 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.480 |
MOD_N-GLC_1 | 214 | 219 | PF02516 | 0.595 |
MOD_N-GLC_1 | 332 | 337 | PF02516 | 0.517 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.534 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.533 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.443 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.514 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.501 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.653 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.555 |
MOD_NEK2_2 | 360 | 365 | PF00069 | 0.485 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.550 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.724 |
MOD_PKA_1 | 55 | 61 | PF00069 | 0.539 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.719 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.430 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.456 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.644 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.443 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.671 |
MOD_Plk_2-3 | 266 | 272 | PF00069 | 0.428 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.565 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.536 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.496 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.688 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.636 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.653 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.586 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.638 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.570 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.527 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.377 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.616 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.570 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.707 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.539 |
TRG_DiLeu_BaEn_1 | 275 | 280 | PF01217 | 0.541 |
TRG_DiLeu_BaEn_2 | 97 | 103 | PF01217 | 0.436 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.543 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8K0 | Leptomonas seymouri | 42% | 100% |
A0A3Q8ISG1 | Leishmania donovani | 68% | 100% |
A4I6G3 | Leishmania infantum | 69% | 100% |
E9B1M0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4Q6J4 | Leishmania major | 70% | 100% |